- Case Report
- Open Access
Dermoid cyst of the mandibula: a case report
© Menditti et al; licensee BioMed Central Ltd. 2008
- Received: 14 October 2008
- Accepted: 22 October 2008
- Published: 22 October 2008
Dermoid cysts are rare congenital lesions derived from pluripotential cells.
We present a case of a female patient aged 30 years presenting for a lesion of the mandibula incidentally seen on a routine panoramic radiograph obtained for dental care. The instrumental, clinical and histological characteristics of the lesion are reported. Finally, a bibliographic revision of this pathology at the level of the oral cavity is reported.
Dermoid cysts must be considered in the differential diagnosis of mandibula's lesions.
- Oral Cavity
- Dental Care
- Squamous Epithelium
- Pluripotential Cell
- Dermoid Cyst
Dermoid cysts are rare congenital lesions derived from pluripotential cells. Nowadays their etiology is unknown. Embriologically, the most reliable theory is that trapped pluripotential cells are a result of the inclusion error, during the early weeks of the intrauterine life, and then they develop into one or into all the three ectoderm, mesoderm and endoderm tissues. The differentiation of these germ layers can produce skin adnexa (such hair, sudoriparous and sebaceous glands), muscle, bone, cartilage, teeth, and mucous membranes. The reason of this occurrence could be any trauma, infection or spontaneous autonomous new growth [1, 2].
Therefore considering these lesions, three varieties may be classified by their histological aspects: epidermoid cyst is lined by stratified squamous epithelium and it's composed of one of the germinal layers (ectodermic); dermoid cyst is lined by stratified epithelium with skin adnexa; teratoid can be cystic or solid featured. In the current literature the term "dermoid cyst" often refers to all types of these lesions [1, 2].
Dermoid cysts are frequently found in sites where embryonic parts fuse together. The majority of reported cases are in the midline of the body, as well as in the ovaries and in the testicles. There is no sex predilection. Their appearance occurs about the second or third decade of life as slowly enlarging masses. The treatment is surgical removal.
In the oral cavity they are also classified as non-odontogenic cystic lesions (accounting for 1,6% of the total); the most frequent sites are the midline of the floor of the mouth (sublingual or submental) and hard palate . Rare cases are reported in the tongue, in the cheek, in the parotid gland and very rare cases in the maxilla and mandibula . They are asymptomatic but their slow enlargement can cause obstruction with consequent dysphagia, dysphonia, and at last dyspnea. The size of dermioid cysts is very variable (up to ten cm in diameter) and it depends on their first clinic manifestation .
We report on a very rare case of epidermoid cyst of the mandibula.
The occurrence of dermoid cysts in the oral cavity is extremely rare [1–5]. Differential diagnosis should include other processes with similar characteristics and situation, such as developmental, neoplastic and infectious diseases. Histological analysis of the excised lesion is always resolutive. In most cases, dermoid cysts are treated by enucleation [6, 7]. Surgical access depends on the location and size of the lesion. In the case presented, the lesion was easily enucleated after intra-oral incision through a "bone window" created by the erosion of the bone of the mandibula. To note, the intra-oral approach leads to good cosmetic and functional results; indeed, the extra-oral approach is mandatory only when the cyst lies under the geniohyoid muscle [6, 7]. Prognosis is good if the cyst has been entirely eliminated; otherwise local recurrence can be observed. Malignant transformation of the dermoid cysts has been reported in some locations, but it has been never described in the mouth [1, 2].
In conclusion, we describe a very rare case of dermoid cyst of the mandibula, successfully diagnosed and managed by surgical excision through intraoral access.
Written informed consent was obtained from the patient for publication of this case report and accompanying images. A copy of the written consent is available for review by the Editor-in-Chief of this journal.
This work was supported by a grant from FUTURA-onlus to AB.
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